Canonical Allele Identifier: CA2774964999

Gene: RP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33096651_33096652insACA , CM000669.2:g.33096651_33096652insACA	GRCh38
NC_000007.13:g.33136263_33136264insACA , CM000669.1:g.33136263_33136264insACA	GRCh37
NC_000007.12:g.33102788_33102789insACA	NCBI36
NG_012968.1:g.17739_17740insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474370.2:n.2379-98_2379-97insTGT
ENST00000492391.2:n.1530-98_1530-97insTGT
ENST00000682645.1:n.3477-98_3477-97insTGT
ENST00000683432.1:c.*581-98_*581-97insTGT	ENSP00000508174.1:n.*581-98_*581-97insTGT
ENST00000684207.1:c.406-98_406-97insTGT	ENSP00000506942.1:n.406-98_406-97insTGT
ENST00000297157.8:c.406-98_406-97insTGT MANE Select	ENSP00000297157.3:n.406-98_406-97insTGT
ENST00000297157.7:c.406-98_406-97insTGT	ENSP00000297157.3:n.406-98_406-97insTGT
ENST00000448915.1:c.304-98_304-97insTGT	ENSP00000411577.1:n.304-98_304-97insTGT
NM_203288.1:c.406-98_406-97insTGT	NP_976033.1:n.406-98_406-97insTGT
XM_011515468.1:c.304-98_304-97insTGT	XP_011513770.1:n.304-98_304-97insTGT
XM_011515468.3:c.304-98_304-97insTGT	XP_011513770.1:n.304-98_304-97insTGT
NM_203288.2:c.406-98_406-97insTGT MANE Select	NP_976033.1:n.406-98_406-97insTGT